Hypoxia-induced switches of myosin heavy chain iso-gene expression in rat heart

被引:41
作者
Razeghi, P
Essop, MF
Huss, JM
Abbasi, S
Manga, N
Taegtmeyer, H
机构
[1] Univ Texas, Houston Med Sch, Dept Internal Med, Div Cardiol, Houston, TX 77030 USA
[2] Univ Cape Town, Sch Med, Hatter Inst Cardiol Res, ZA-7925 Cape Town, South Africa
[3] Washington Univ, Sch Med, Cardiovasc Res Ctr, St Louis, MO USA
关键词
hypoxia; fetal gene program; MHC iso-genes; quantitative RT-PCR;
D O I
10.1016/S0006-291X(03)00478-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cardiac hypertrophy and atrophy increase expression of fetal iso-genes. A common factor is a decrease in cellular oxygen tension. To test the hypothesis that hypoxia changes cardiac MHC iso-gene expression Wistar rats were exposed to 24 and 48 It of hypobaric hypoxia (11% oxygen) and mRNA was isolated from the left ventricle. In addition, neonatal rat cardiomyocytes were incubated for up to 48 h in a hypoxic chamber. Transcript levels of MHCalpha (adult isoform), MHCbeta (fetal isoform), and Nkx2.5, the earliest known marker for cardiogenesis, were measured by real-time quantitative RT-PCR and normalized to levels of I SS rRNA. Expression of the transcription factor Nkx2.5 increased with hypoxia. Hypoxia decreased MHCalpha and increased MHCbeta transcript levels, both in vivo and in vitro. We conclude that hypoxia per se induces a pattern of isoform gene expression associated with early cardiac development. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1024 / 1027
页数:4
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